Cell-type and tissue-specific expression of caveolin-2. Caveolins 1 and 2 co-localize and form a stable hetero-oligomeric complex in vivo
Caveolae are microdomains of the plasma membrane that have been implicated in organizing and compartmentalizing signal transducing molecules. Caveolin, a 21-24-kDa integral membrane protein, is a principal structural component of caveolae membrane in vivo. Recently, we and other laboratories have id...
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Veröffentlicht in: | The Journal of biological chemistry 1997-11, Vol.272 (46), p.29337-29346 |
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description | Caveolae are microdomains of the plasma membrane that have been implicated in organizing and compartmentalizing signal transducing molecules. Caveolin, a 21-24-kDa integral membrane protein, is a principal structural component of caveolae membrane in vivo. Recently, we and other laboratories have identified a family of caveolin-related proteins; caveolin has been re-termed caveolin-1. Here, we examine the cell-type and tissue-specific expression of caveolin-2. For this purpose, we generated a novel mono-specific monoclonal antibody probe that recognizes only caveolin-2, but not caveolins-1 and -3. A survey of cell and tissue types demonstrates that the caveolin-2 protein is most abundantly expressed in endothelial cells, smooth muscle cells, skeletal myoblasts (L6, BC3H1, C2C12), fibroblasts, and 3T3-L1 cells differentiated to adipocytes. This pattern of caveolin-2 protein expression most closely resembles the cellular distribution of caveolin-1. In line with these observations, co-immunoprecipitation experiments with mono-specific antibodies directed against either caveolin-1 or caveolin-2 directly show that these molecules form a stable hetero-oligomeric complex. The in vivo relevance of this complex was further revealed by dual-labeling studies employing confocal laser scanning fluorescence microscopy. Our results indicate that caveolins 1 and 2 are strictly co-localized within the plasma membrane and other internal cellular membranes. Ultrastructurally, this pattern of caveolin-2 localization corresponds to caveolae membranes as seen by immunoelectron microscopy. Despite this strict co-localization, it appears that regulation of caveolin-2 expression occurs independently of the expression of either caveolin-1 or caveolin-3 as observed using two different model cell systems. Although caveolin-1 expression is down-regulated in response to oncogenic transformation of NIH 3T3 cells, caveolin-2 protein levels remain unchanged. Also, caveolin-2 protein levels remain unchanged during the differentiation of C2C12 cells from myoblasts to myotubes, while caveolin-3 levels are dramatically induced by this process. These results suggest that expression levels of caveolins 1, 2, and 3 can be independently up-regulated or down-regulated in response to a variety of distinct cellular cues. |
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Here, we examine the cell-type and tissue-specific expression of caveolin-2. For this purpose, we generated a novel mono-specific monoclonal antibody probe that recognizes only caveolin-2, but not caveolins-1 and -3. A survey of cell and tissue types demonstrates that the caveolin-2 protein is most abundantly expressed in endothelial cells, smooth muscle cells, skeletal myoblasts (L6, BC3H1, C2C12), fibroblasts, and 3T3-L1 cells differentiated to adipocytes. This pattern of caveolin-2 protein expression most closely resembles the cellular distribution of caveolin-1. In line with these observations, co-immunoprecipitation experiments with mono-specific antibodies directed against either caveolin-1 or caveolin-2 directly show that these molecules form a stable hetero-oligomeric complex. The in vivo relevance of this complex was further revealed by dual-labeling studies employing confocal laser scanning fluorescence microscopy. Our results indicate that caveolins 1 and 2 are strictly co-localized within the plasma membrane and other internal cellular membranes. Ultrastructurally, this pattern of caveolin-2 localization corresponds to caveolae membranes as seen by immunoelectron microscopy. Despite this strict co-localization, it appears that regulation of caveolin-2 expression occurs independently of the expression of either caveolin-1 or caveolin-3 as observed using two different model cell systems. Although caveolin-1 expression is down-regulated in response to oncogenic transformation of NIH 3T3 cells, caveolin-2 protein levels remain unchanged. Also, caveolin-2 protein levels remain unchanged during the differentiation of C2C12 cells from myoblasts to myotubes, while caveolin-3 levels are dramatically induced by this process. 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Caveolins 1 and 2 co-localize and form a stable hetero-oligomeric complex in vivo</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Caveolae are microdomains of the plasma membrane that have been implicated in organizing and compartmentalizing signal transducing molecules. Caveolin, a 21-24-kDa integral membrane protein, is a principal structural component of caveolae membrane in vivo. Recently, we and other laboratories have identified a family of caveolin-related proteins; caveolin has been re-termed caveolin-1. Here, we examine the cell-type and tissue-specific expression of caveolin-2. For this purpose, we generated a novel mono-specific monoclonal antibody probe that recognizes only caveolin-2, but not caveolins-1 and -3. A survey of cell and tissue types demonstrates that the caveolin-2 protein is most abundantly expressed in endothelial cells, smooth muscle cells, skeletal myoblasts (L6, BC3H1, C2C12), fibroblasts, and 3T3-L1 cells differentiated to adipocytes. This pattern of caveolin-2 protein expression most closely resembles the cellular distribution of caveolin-1. In line with these observations, co-immunoprecipitation experiments with mono-specific antibodies directed against either caveolin-1 or caveolin-2 directly show that these molecules form a stable hetero-oligomeric complex. The in vivo relevance of this complex was further revealed by dual-labeling studies employing confocal laser scanning fluorescence microscopy. Our results indicate that caveolins 1 and 2 are strictly co-localized within the plasma membrane and other internal cellular membranes. Ultrastructurally, this pattern of caveolin-2 localization corresponds to caveolae membranes as seen by immunoelectron microscopy. Despite this strict co-localization, it appears that regulation of caveolin-2 expression occurs independently of the expression of either caveolin-1 or caveolin-3 as observed using two different model cell systems. Although caveolin-1 expression is down-regulated in response to oncogenic transformation of NIH 3T3 cells, caveolin-2 protein levels remain unchanged. Also, caveolin-2 protein levels remain unchanged during the differentiation of C2C12 cells from myoblasts to myotubes, while caveolin-3 levels are dramatically induced by this process. These results suggest that expression levels of caveolins 1, 2, and 3 can be independently up-regulated or down-regulated in response to a variety of distinct cellular cues.</description><subject>3T3 Cells</subject><subject>Adipocytes - cytology</subject><subject>Adipocytes - metabolism</subject><subject>Animals</subject><subject>Biopolymers</subject><subject>Caveolin 1</subject><subject>Caveolin 2</subject><subject>Caveolins</subject><subject>Cell Line, Transformed</subject><subject>Cell Membrane - metabolism</subject><subject>Humans</subject><subject>Intracellular Membranes - metabolism</subject><subject>Intracellular Membranes - ultrastructure</subject><subject>Membrane Proteins - biosynthesis</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice</subject><subject>Microscopy, Immunoelectron</subject><subject>Molecular Sequence Data</subject><issn>0021-9258</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotkD1PwzAYhD2ASinsLEie2Bz81SQeUcWXVIkF5sixX4MrJw5xUrX8A_41Ec0td8PdMxxCN4xmjBbyflebjBc8k3nGlRDFGVpSyhlRfF1eoMuUdnSSVGyBFkrkjLL1Ev1uIAQyHDvAurV48CmNQFIHxjtvMBy6HlLyscXRYaP3EINvCc_wZs4Js_8lxyaSEI0O_ufEcrFvsMZp0HUA_AUD9JFMk8_YQD-xTWy6AAfsW7z3-3iFzp0OCa5nX6GPp8f3zQvZvj2_bh62pOO0HIjm1EBeWu2srA1Iy0qllM6BSS4oz0UpbG60ddIJyQsnhC2KfM0Mk4UzVIkVujtxuz5-j5CGqvHJTC_oFuKYqkJJWtIJtkK3c3GsG7BV1_tG98dq_k78AfwwcGk</recordid><startdate>19971114</startdate><enddate>19971114</enddate><creator>Scherer, P E</creator><creator>Lewis, R Y</creator><creator>Volonte, D</creator><creator>Engelman, J A</creator><creator>Galbiati, F</creator><creator>Couet, J</creator><creator>Kohtz, D S</creator><creator>van Donselaar, E</creator><creator>Peters, P</creator><creator>Lisanti, M P</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19971114</creationdate><title>Cell-type and tissue-specific expression of caveolin-2. Caveolins 1 and 2 co-localize and form a stable hetero-oligomeric complex in vivo</title><author>Scherer, P E ; Lewis, R Y ; Volonte, D ; Engelman, J A ; Galbiati, F ; Couet, J ; Kohtz, D S ; van Donselaar, E ; Peters, P ; Lisanti, M P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p208t-a20ce68dafd4bce4d18999a6e1423026383d6cadf4f3427f33d77651c147fc093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>3T3 Cells</topic><topic>Adipocytes - cytology</topic><topic>Adipocytes - metabolism</topic><topic>Animals</topic><topic>Biopolymers</topic><topic>Caveolin 1</topic><topic>Caveolin 2</topic><topic>Caveolins</topic><topic>Cell Line, Transformed</topic><topic>Cell Membrane - metabolism</topic><topic>Humans</topic><topic>Intracellular Membranes - metabolism</topic><topic>Intracellular Membranes - ultrastructure</topic><topic>Membrane Proteins - biosynthesis</topic><topic>Membrane Proteins - metabolism</topic><topic>Mice</topic><topic>Microscopy, Immunoelectron</topic><topic>Molecular Sequence Data</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scherer, P E</creatorcontrib><creatorcontrib>Lewis, R Y</creatorcontrib><creatorcontrib>Volonte, D</creatorcontrib><creatorcontrib>Engelman, J A</creatorcontrib><creatorcontrib>Galbiati, F</creatorcontrib><creatorcontrib>Couet, J</creatorcontrib><creatorcontrib>Kohtz, D S</creatorcontrib><creatorcontrib>van Donselaar, E</creatorcontrib><creatorcontrib>Peters, P</creatorcontrib><creatorcontrib>Lisanti, M P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scherer, P E</au><au>Lewis, R Y</au><au>Volonte, D</au><au>Engelman, J A</au><au>Galbiati, F</au><au>Couet, J</au><au>Kohtz, D S</au><au>van Donselaar, E</au><au>Peters, P</au><au>Lisanti, M P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell-type and tissue-specific expression of caveolin-2. Caveolins 1 and 2 co-localize and form a stable hetero-oligomeric complex in vivo</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1997-11-14</date><risdate>1997</risdate><volume>272</volume><issue>46</issue><spage>29337</spage><epage>29346</epage><pages>29337-29346</pages><issn>0021-9258</issn><abstract>Caveolae are microdomains of the plasma membrane that have been implicated in organizing and compartmentalizing signal transducing molecules. Caveolin, a 21-24-kDa integral membrane protein, is a principal structural component of caveolae membrane in vivo. Recently, we and other laboratories have identified a family of caveolin-related proteins; caveolin has been re-termed caveolin-1. Here, we examine the cell-type and tissue-specific expression of caveolin-2. For this purpose, we generated a novel mono-specific monoclonal antibody probe that recognizes only caveolin-2, but not caveolins-1 and -3. A survey of cell and tissue types demonstrates that the caveolin-2 protein is most abundantly expressed in endothelial cells, smooth muscle cells, skeletal myoblasts (L6, BC3H1, C2C12), fibroblasts, and 3T3-L1 cells differentiated to adipocytes. This pattern of caveolin-2 protein expression most closely resembles the cellular distribution of caveolin-1. In line with these observations, co-immunoprecipitation experiments with mono-specific antibodies directed against either caveolin-1 or caveolin-2 directly show that these molecules form a stable hetero-oligomeric complex. The in vivo relevance of this complex was further revealed by dual-labeling studies employing confocal laser scanning fluorescence microscopy. Our results indicate that caveolins 1 and 2 are strictly co-localized within the plasma membrane and other internal cellular membranes. Ultrastructurally, this pattern of caveolin-2 localization corresponds to caveolae membranes as seen by immunoelectron microscopy. Despite this strict co-localization, it appears that regulation of caveolin-2 expression occurs independently of the expression of either caveolin-1 or caveolin-3 as observed using two different model cell systems. Although caveolin-1 expression is down-regulated in response to oncogenic transformation of NIH 3T3 cells, caveolin-2 protein levels remain unchanged. Also, caveolin-2 protein levels remain unchanged during the differentiation of C2C12 cells from myoblasts to myotubes, while caveolin-3 levels are dramatically induced by this process. These results suggest that expression levels of caveolins 1, 2, and 3 can be independently up-regulated or down-regulated in response to a variety of distinct cellular cues.</abstract><cop>United States</cop><pmid>9361015</pmid><doi>10.1074/jbc.272.46.29337</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3T3 Cells Adipocytes - cytology Adipocytes - metabolism Animals Biopolymers Caveolin 1 Caveolin 2 Caveolins Cell Line, Transformed Cell Membrane - metabolism Humans Intracellular Membranes - metabolism Intracellular Membranes - ultrastructure Membrane Proteins - biosynthesis Membrane Proteins - metabolism Mice Microscopy, Immunoelectron Molecular Sequence Data |
title | Cell-type and tissue-specific expression of caveolin-2. Caveolins 1 and 2 co-localize and form a stable hetero-oligomeric complex in vivo |
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